# ETOMIDATE

NDC: 55150-222
Generic name: ETOMIDATE
Labeler / Manufacturer: Eugia US LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20170224

FDA application: ANDA206126

## Active ingredients

- ETOMIDATE: 40 mg/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55150-222"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55150-222
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0820f15a-046b-4185-a2b3-2e4051ee3d82